Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18084생성일: 2026년 10월 24일
tert-Butyl (2S)-2-(aminomethyl)piperidine-1-carboxylate → (S)-2-[(6,7-Difluoro-3-methylquinoxaline-2-ylamino)methyl]-piperidine-1-carboxylic acid tert butylester
https://huagongshe.com/ko/reaction/18084
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | tert-Butyl (2S)-2-(aminomethyl)piperidine-1-carboxylate | HCID 1502020 | — |
| 반응물 | 2-Chloro-6,7-difluoro-3-methylquinoxaline | HCID 10220011 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (S)-2-[(6,7-Difluoro-3-methylquinoxaline-2-ylamino)methyl]-piperidine-1-carboxylic acid tert butylester | HCID 86593671 | — |
반응 단계
(S)-2-Aminomethyl-piperidine-1-carboxylic acid tert-butyl ester (1.14 g), and 2-chloro-6,7-difluoro-3-methylquinoxaline Teng et al PCT Int. Appl (2000), WO00/42026A1 20000720 (1.14 g) were dissolved in DMF (2 ml) and heated to 90° C. for 3 days under an atmosphere of argon. After cooling, the reaction solution was partitioned between ethyl acetate and water. The organic layer was washed with water, saturated brine, dried and evaporated. The residue was chromatographed over silica gel, eluting with a gradient of 10 to 50% ethyl acetate in hexane. The title compound was obtained as a pink foam (0.524 g), MH+ 393.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07741329B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-e387087c8a394279bd035d0d571cc60a |
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| 출처 메모 | uspto-grants-2010_06 |
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